1. Use standard conventions to write a mechanism for the reaction sequence below and provide an...
1. Write a structural formula for each of the following compounds: (36 pts) (a) m-chlorobenzoyl chloride (b) N-ethyl benzamide (c) dibenzalacetone (d) ethyl acetoacetate (e) 2-ethyl-1-butanamine (t) dibenzylamine 2. Write a structural formula for the principal organic product or products of each of the following reactions: (36 pts) (a) propanoyl chloride and sodium propanoate (b) acetic anhydride and 3-pentanol (c) acetaldehyde and sodium ethoxide (CH3CH2ONa) in ethanol solvent (d) cyclohexanone, benzaldehyde, and NaOH (e) 2-aminopropane and acetyl chloride in pyridine...
Write the product and a complete arrow-pushing mechanism and propose (the) major product(s) for the following transformation. After a Grignard reaction. .... Each of the Grignard reactions we have studied so far produces an alcohol as the major organic product. Alcohols can be used as starting materials for a number of organic reactions. Use this exercise to consider the range of reactions that can be performed after a Grignard reaction. For each reaction sequence below, suggest a Grignard reagent and...
Provide a sequence of reaction to convert the starting material to the product. Show all reagents and synthetic intermediates. You can use any addition carbon sources if needed but you must use the starting material given. The mechanisms do not have to be shown. Synthesis 1. The following transformations cannot be perfor Uwing transformations cannot be performed in one step. Provide a sequence of reactions 10 convert the "starting material" to the "product." Show all the reagents and synthetic intermediates....
1. The following transformations cannot be performed in one step. Provide a sequence of reactions to convert the "starting material to the product." Show all the reagents and synthetic intermediates. You can use any additional carbon sources if needed, but you must use the starting material given.
1. The following transformations cannot be performed in one step. Provide a sequence of reactions to convert the "starting material" to the "product." Show all the reagents and synthetic intermediates. You can use any additional carbon sources if needed, but you must use the starting material given. H
1. The following transformations cannot be performed in one step. Provide a sequence of reactions to convert the starting material to the product. Show all the reagents and synthetic intermediates. You can use any additional carbon sources if needed, but you must use the starting material given. OH он
1. The following transformations cannot be performed in one step. Provide a sequence of reactions to convert the "starting material" to the "product." Show all the reagents and synthetic intermediates. You can use any additional carbon sources if needed, but you must use the starting material given. Hot Br
Synthesis 1. The following transformations cannot be performed in one step. Provide a sequence of reactions to convert the "starting material to the "product." Show all the reagents and synthetic intermediates. You can use any additional carbon sources if needed, but you must use the starting material given
1. The following transformatioms cannot be performed in one step. Provide a sequence of reactions to convert the "starting material" to the "product". Show all the reagents and synthetic intermediates. You can ise any additional carbon sources of needed, but you must use the starting material given. Br СОН -
1. The following transformations cannot be performed in one step. Provide a sequence of reactions to convert the "starting material to the product." Show all the reagents and synthetic intermediates. You can use any additional carbon sources if needed, but you must use the starting material given. CN